Canonical Allele Identifier: CA2574605815

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290581

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965502C>G , CM000672.2:g.87965502C>G	GRCh38
NC_000010.10:g.89725259C>G , CM000672.1:g.89725259C>G	GRCh37
NC_000010.9:g.89715239C>G	NCBI36
NG_007466.2:g.107064C>G , LRG_311:g.107064C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*30C>G	ENSP00000514759.2:n.*30C>G
ENST00000710265.1:c.*271C>G	ENSP00000518161.1:n.*271C>G
ENST00000688158.2:n.1977C>G
ENST00000688922.2:c.*1072C>G	ENSP00000508742.2:n.*1072C>G
ENST00000700021.1:c.*30C>G	ENSP00000514757.1:n.*30C>G
ENST00000700022.1:c.*581C>G	ENSP00000514758.1:n.*581C>G
ENST00000700023.1:n.2400C>G
ENST00000700024.1:n.2634C>G
ENST00000706954.1:c.*30C>G	ENSP00000516674.1:n.*30C>G
ENST00000706955.1:c.*1277C>G	ENSP00000516675.1:n.*1277C>G
ENST00000686459.1:c.*828C>G	ENSP00000508909.1:n.*828C>G
ENST00000688158.1:c.*1353C>G	ENSP00000509254.1:n.*1353C>G
ENST00000688308.1:c.*30C>G	ENSP00000508752.1:n.*30C>G
ENST00000688922.1:c.1163C>G
ENST00000693560.1:c.*30C>G	ENSP00000509861.1:n.*30C>G
ENST00000371953.8:c.*30C>G MANE Select	ENSP00000361021.3:n.*30C>G
ENST00000371953.7:c.*30C>G	ENSP00000361021.3:n.*30C>G
NM_000314.5:c.*30C>G	NP_000305.3:n.*30C>G
NM_000314.6:c.*30C>G	NP_000305.3:n.*30C>G
NM_001304717.2:c.*30C>G	NP_001291646.2:n.*30C>G
NM_001304718.1:c.*30C>G	NP_001291647.1:n.*30C>G
XM_006717926.2:c.*30C>G	XP_006717989.1:n.*30C>G
XM_011539982.1:c.*30C>G	XP_011538284.1:n.*30C>G
XR_945791.1:n.1812C>G
NM_000314.7:c.*30C>G	NP_000305.3:n.*30C>G
NM_001304717.5:c.*30C>G	NP_001291646.4:n.*30C>G
NM_001304718.2:c.*30C>G	NP_001291647.1:n.*30C>G
NM_000314.8:c.*30C>G MANE Select	NP_000305.3:n.*30C>G